| Name |
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TIMM44 Genetranslocase of inner mitochondrial membrane 44 homolog (yeast) This gene encodes a peripheral membrane protein associated with the mitochondrial inner membrane translocase, which functions in the import of proteins across the mitochondrial inner membrane and into the mitochondrial matrix. The encoded protein mediates binding of mitochondrial heat shock protein 70 to the translocase of inner mitochondrial membrane 23 (TIM23) complex. Expression of this gene is upregulated in kidney in a mouse model of diabetes. A mutation in this gene is associated with familial oncocytic thyroid carcinoma. [provided by RefSeq, Jul 2016] |
OPALIN Geneoligodendrocytic myelin paranodal and inner loop protein Predicted to be involved in regulation of oligodendrocyte differentiation. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
TIMM8BP1 Genetranslocase of inner mitochondrial membrane 8B pseudogene 1 |
IMMP2L GeneIMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) This gene encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for this gene. [provided by RefSeq, Sep 2011] |
TIMM17BP1 Genetranslocase of inner mitochondrial membrane 17 homolog B (yeast) pseudogene 1 |
MPV17 GeneMpV17 mitochondrial inner membrane protein This gene encodes a mitochondrial inner membrane protein that is implicated in the metabolism of reactive oxygen species. Mutations in this gene have been associated with the hepatocerebral form of mitochondrial DNA depletion syndrome (MDDS). [provided by RefSeq, Jul 2008] |
INCENP Geneinner centromere protein antigens 135/155kDa In mammalian cells, 2 broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and 'passenger,' or transiently interacting, proteins (reviewed by Choo, 1997). The constitutive proteins include CENPA (centromere protein A; MIM 117139), CENPB (MIM 117140), CENPC1 (MIM 117141), and CENPD (MIM 117142). The term 'passenger proteins' encompasses a broad collection of proteins that localize to the centromere during specific stages of the cell cycle (Earnshaw and Mackay, 1994 [PubMed 8088460]). These include CENPE (MIM 117143); MCAK (MIM 604538); KID (MIM 603213); cytoplasmic dynein (e.g., MIM 600112); CliPs (e.g., MIM 179838); and CENPF/mitosin (MIM 600236). The inner centromere proteins (INCENPs) (Earnshaw and Cooke, 1991 [PubMed 1860899]), the initial members of the passenger protein group, display a broad localization along chromosomes in the early stages of mitosis but gradually become concentrated at centromeres as the cell cycle progresses into mid-metaphase. During telophase, the proteins are located within the midbody in the intercellular bridge, where they are discarded after cytokinesis (Cutts et al., 1999 [PubMed 10369859]).[supplied by OMIM, Mar 2008] |
TIMM10B Genetranslocase of inner mitochondrial membrane 10 homolog B (yeast) FXC1, or TIMM10B, belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004] |
TIMM50 Genetranslocase of inner mitochondrial membrane 50 homolog (S. cerevisiae) This gene encodes a subunit of the TIM23 inner mitochondrial membrane translocase complex. The encoded protein functions as the receptor subunit that recognizes the mitochondrial targeting signal, or presequence, on protein cargo that is destined for the mitochondrial inner membrane and matrix. This protein may also play a role in maintaining the membrane permeability barrier, and knockdown of this gene in human cells results in the release of cytochrome c and apoptosis. [provided by RefSeq, Jul 2016] |
MINOS1P4 Genemitochondrial inner membrane organizing system 1 pseudogene 4 |
IMMP1LP1 GeneIMP1 inner mitochondrial membrane peptidase-like (S. cerevisiae) pseudogene 1 |
TIMM8A Genetranslocase of inner mitochondrial membrane 8 homolog A (yeast) This translocase is involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS) and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in this gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. This protein, along with TIMM13, forms a 70 kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Mar 2009] |
TIMM8B Genetranslocase of inner mitochondrial membrane 8 homolog B (yeast) This gene encodes a member of a well-conserved family of proteins with similarity to yeast Tim mitochondrial import proteins. This gene is encoded by a nuclear gene and is transported into the intermembrane space of the mitochondrion. When formed into complexes, these proteins guide membrane-spanning proteins across the mitochondrial intermembrane space before they are added into the mitochondrial inner membrane. This gene is adjacent to succinate dehydrogenase, subunit D (SDHD), in which mutations have been found in affected members of families with hereditary paraganglioma.[provided by RefSeq, Aug 2009] |
TIMMDC1 Genetranslocase of inner mitochondrial membrane domain containing 1 Predicted to be involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion and nucleoplasm. Implicated in nuclear type mitochondrial complex I deficiency 31. [provided by Alliance of Genome Resources, Mar 2025] |
TIMM9 Genetranslocase of inner mitochondrial membrane 9 homolog (yeast) TIMM9 belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004] |
MINOS1P3 Genemitochondrial inner membrane organizing system 1 pseudogene 3 |
MINOS1P2 Genemitochondrial inner membrane organizing system 1 pseudogene 2 |
MINOS1P1 Genemitochondrial inner membrane organizing system 1 pseudogene 1 |
MINOS1 Genemitochondrial inner membrane organizing system 1 Involved in cristae formation. Located in mitochondrion. Part of MIB complex; MICOS complex; and SAM complex. [provided by Alliance of Genome Resources, Mar 2025] |
IMMT Geneinner membrane protein, mitochondrial Enables RNA binding activity. Involved in cristae formation. Located in mitochondrial inner membrane. Part of MICOS complex. [provided by Alliance of Genome Resources, Mar 2025] |
IMMTP1 Geneinner membrane protein, mitochondrial (mitofilin) pseudogene 1 |
TIMM23 Genetranslocase of inner mitochondrial membrane 23 homolog (yeast) The protein encoded by this gene is part of a complex located in the inner mitochondrial membrane that mediates the transport of transit peptide-containing proteins across the membrane. Multiple transcript variants, one protein-coding and others not protein-coding, have been found for this gene. [provided by RefSeq, Jul 2012] |
TIMM22 Genetranslocase of inner mitochondrial membrane 22 homolog (yeast) Multipass transmembrane proteins are brought into mitochondria and inserted into the mitochondrial inner membrane by way of the TIM22 complex. This complex has six subunits and is a twin-pore translocase. The protein encoded by this gene is a subunit of TIM22 and represents the voltage-activated and signal-gated channel. [provided by RefSeq, Jul 2016] |
TIMM17B Genetranslocase of inner mitochondrial membrane 17 homolog B (yeast) This gene encodes a multipass transmembrane protein that forms an integral component of the mitochondrial translocase TIM23 complex. This complex facilitates the transport of mitochondrial proteins from the cytosol across the mitochondrial inner membrane and into the mitochondrion. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
TIMM17A Genetranslocase of inner mitochondrial membrane 17 homolog A (yeast) Predicted to contribute to protein transmembrane transporter activity. Predicted to be involved in protein import into mitochondrial matrix. Located in mitochondrial inner membrane and nucleoplasm. Part of TIM23 mitochondrial import inner membrane translocase complex. [provided by Alliance of Genome Resources, Mar 2025] |
IMMP1L GeneIMP1 inner mitochondrial membrane peptidase-like (S. cerevisiae) The mitochondrial inner membrane peptidase (IMP) complex generates mature, active proteins in the mitochondrial intermembrane space by proteolytically removing the mitochondrial targeting presequence of nuclear-encoded proteins. IMP1 and IMP2 (IMMP2L; MIM 605977) are the catalytic subunits of the IMP complex (Burri et al., 2005 [PubMed 15814844]).[supplied by OMIM, Sep 2008] |
TMIE Genetransmembrane inner ear This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment. [provided by RefSeq, Mar 2009] |
TIMM8BP2 Genetranslocase of inner mitochondrial membrane 8B pseudogene 2 |
TIMM13 Genetranslocase of inner mitochondrial membrane 13 homolog (yeast) This gene encodes a member of the evolutionarily conserved TIMM (translocase of inner mitochondrial membrane) family of proteins that function as chaperones in the import of proteins from the cytoplasm into the mitochondrial inner membrane. Proteins of this family play a role in collecting substrate proteins from the translocase of the outer mitochondrial membrane (TOM) complex and delivering them to either the sorting and assembly machinery in the outer mitochondrial membrane (SAM) complex or the TIMM22 complex in the inner mitochondrial membrane. The encoded protein and the translocase of mitochondrial inner membrane 8a protein form a 70 kDa complex in the intermembrane space. [provided by RefSeq, Jul 2013] |
TIMM10 Genetranslocase of inner mitochondrial membrane 10 homolog (yeast) The mitochondrial protein encoded by this gene belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane, functioning as intermembrane space chaperones for the highly insoluble carrier proteins. [provided by RefSeq, Nov 2011] |
TIMM21 Genetranslocase of inner mitochondrial membrane 21 homolog (yeast) Involved in mitochondrial cytochrome c oxidase assembly; mitochondrial respiratory chain complex I assembly; and protein import into mitochondrial matrix. Located in mitochondrion. Part of TIM23 mitochondrial import inner membrane translocase complex. [provided by Alliance of Genome Resources, Mar 2025] |
IMMP1LP2 GeneIMP1 inner mitochondrial membrane peptidase-like (S. cerevisiae) pseudogene 2 |
TIMM8AP1 Genetranslocase of inner mitochondrial membrane 8 homolog A (yeast) pseudogene 1 |
LOC105369987 Genemitochondrial inner membrane protease subunit 1 pseudogene |
TIMM23B Genetranslocase of inner mitochondrial membrane 23 homolog B (yeast) Predicted to enable protein transmembrane transporter activity. Predicted to be involved in protein import into mitochondrial matrix. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
TIMM29 Genetranslocase of inner mitochondrial membrane 29 Enables protein transporter activity. Involved in protein insertion into mitochondrial inner membrane. Located in mitochondrial inner membrane and mitochondrial intermembrane space. Part of TIM22 mitochondrial import inner membrane insertion complex. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP3 Genesperm microtubule inner protein 3 |
CIMIP3 Geneciliary microtubule inner protein 3 Predicted to enable calcium ion binding activity. Predicted to be involved in visual perception. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP8 Genesperm microtubule inner protein 8 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and motile cilium. Predicted to be active in axonemal A tubule inner sheath and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
CIMIP7 Geneciliary microtubule inner protein 7 |
CIMIP2C Geneciliary microtubule inner protein 2C Predicted to be involved in flagellated sperm motility. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Mar 2025] |
CIMIP4 Geneciliary microtubule inner protein 4 Predicted to be located in sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
CIMIP2A Geneciliary microtubule inner protein 2A Predicted to be involved in flagellated sperm motility. Located in ciliary basal body. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP6 Genesperm microtubule inner protein 6 This gene encodes a nuclear- or perinuclear-localized protein with no predicted domains or similarity to other known proteins. Expression of this gene is induced during the differentiation of bronchial epithelial cells, and the encoded protein may play a role in ciliogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
CIMIP1 Geneciliary microtubule inner protein 1 Located in cilium. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP2 Genesperm microtubule inner protein 2 |
SPMIP9 Genesperm microtubule inner protein 9 Predicted to be involved in flagellated sperm motility. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP7 Genesperm microtubule inner protein 7 Predicted to be involved in spermatogenesis. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP5 Genesperm microtubule inner protein 5 Predicted to be involved in flagellated sperm motility. Predicted to be located in several cellular components, including cytoskeleton; motile cilium; and nucleus. Predicted to be active in axonemal A tubule inner sheath and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP10 Genesperm microtubule inner protein 10 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and motile cilium. Predicted to be active in axonemal B tubule inner sheath and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP1 Genesperm microtubule inner protein 1 |
SPMIP11 Genesperm microtubule inner protein 11 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and sperm flagellum. Predicted to be active in axonemal A tubule inner sheath. [provided by Alliance of Genome Resources, Mar 2025] |
CIMIP2B Geneciliary microtubule inner protein 2B Predicted to be involved in flagellated sperm motility. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Mar 2025] |
SPMIP4 Genesperm microtubule inner protein 4 |
MIMS2 Genemitochondrial inner membrane scaffold 2 |
MIMS1 Genemitochondrial inner membrane scaffold 1 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
MNMIP1 Genemanchette microtubule inner protein 1 Predicted to be involved in actin filament organization and cell migration. Located in nucleoplasm and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MISO1 Genemitochondrial inner membrane subdomain organizer 1 Involved in negative regulation of ERK1 and ERK2 cascade and regulation of DNA-binding transcription factor activity. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |